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NCT01801202 · ClinicalTrials.gov registry record · NA
Clinical Evaluation of LightSheer Duet 805nm HS Handpiece
A NA study, sponsored by Lumenis Be.
- Completed
- Registry status
- NA
- Development phase
- 21
- Enrollment target
NCT01801202 is a NA study that has completed, run by Lumenis Be. The registered enrollment target is 21 participants.
The verdict
NCT01801202, a NA study, has completed, sponsored by Lumenis Be.
- COMPLETED
- Registry status
- NA
- Development phase
- 21 participants
- Enrollment target
Study Summary
* The study will re-confirm that the LightSheer Duet HS 805 nm handpiece is safe for removal of unwanted hair, and will result in hair removal and permanent hair count reduction. * Twenty (20)subjects, Fitzpatrick Skin Type I-IV will be included in a single site. * Each subject will receive five treatments at four to six week intervals and return for follow-up visits at three and six months after the last treatment for evaluation of the treated areas.
Interventions
- DEVICE LightSheer Duet HS handpiece
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2013-02 |
| Est. Completion | 2014-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01801202
The ClinicalTrials.gov registry entry for NCT01801202 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Lumenis Be, which has 20 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which LightSheer Duet HS handpiece is the first listed.
NCT01801202 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01801202 about?
NCT01801202 is a clinical study titled "Clinical Evaluation of LightSheer Duet 805nm HS Handpiece". * The study will re-confirm that the LightSheer Duet HS 805 nm handpiece is safe for removal of unwanted hair, and will result in hair removal and permanent hair count reduction. * Twenty (20)subjects, Fitzpatrick Skin Type I-IV will be included in a single site. * Each subject will receive five tre...
What is the current status of trial NCT01801202?
This trial is currently completed. It is a NA study. The enrollment target is 21 participants. The study started on 2013-02. Estimated completion is 2014-11.
What interventions are being tested in trial NCT01801202?
The interventions under investigation include: LightSheer Duet HS handpiece (DEVICE).
Who is sponsoring clinical trial NCT01801202?
This trial is sponsored by Lumenis Be, which has 20 total clinical trials registered on ClinicalTrials.gov.
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